Poor growth of human adenovirus-12 compared to adenovirus-2 correlates with a failure to impair PKR activation during the late phase of infection

被引:3
作者
Wu, Chengjun [1 ]
Bai, Lufeng [1 ]
Li, Zhiqun [2 ]
Samuel, Charles E. [2 ]
Akusjarvi, Goran [1 ]
Svensson, Catharina [1 ]
机构
[1] Uppsala Univ, Dept Med Biochem & Microbiol, S-75123 Uppsala, Sweden
[2] Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USA
基金
瑞典研究理事会;
关键词
Adenovirus; VA RNA; IFN; PKR; eIF2; alpha; INTERFERON REGULATORY FACTOR-3; VIRUS-ASSOCIATED RNA; PROTEIN-KINASE PKR; VAI RNA; GENE-EXPRESSION; MESSENGER-RNA; E1A PROTEINS; I INTERFERON; TRANSLATION; INDUCTION;
D O I
10.1016/j.virol.2014.11.012
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human adenovirus type 12 (HAdV-12) displays a relatively low virulence and slow replication in cultured human cells, which is manifested by premature death of HAdV-12-infected cells. Whereas HAdV-2 induction of IFN-beta expression was transient, HAdV-12-infected cells maintained high levels of IFN-beta expression, protein kinase R (PKR) activation and eIF-2 alpha phosphorylation throughout the infectious cycle. The importance of the IFN-inducible PKR kinase in restriction of HAdV-12 was supported by the enhanced growth of the virus following PKR knockdown in HeLa cells. Ectopic expression of HAdV-2 VA RNAI increased HAdV-12 hexon protein expression, suggesting that insufficient VA RNA expression contributes to the restricted growth of HAdV-12. Although some adenovirus species are known to persist in human lymphoid tissues, HAdV12 has so far not been found. Thus, it is possible that the inability of HAdV12 to evade the INF response may have implications for the virus to establish long-lasting or persistent infections. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:120 / 128
页数:9
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